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Home >Products> Reagents >Antibody> Invivo anti-mouse PD-L1 Recombinant mAb (D265A)
Invivo anti-mouse PD-L1 Recombinant mAb (D265A)
Invivo anti-mouse PD-L1 Recombinant mAb (D265A)
Origin of place Singapore
Model S0B0593-1mg
Supplier ANT BIO PTE.LTD.
Price 120
Hits 2
Updated 8/27/2025
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Product Specification


HostMouse
AntigenPD-L1
SynonymsProgrammed cell death 1 ligand 1, CD274, B7-H1
LocationMembrane
AccessionQ9EP73
Clone Number10F.9G2
Antibody TypeRecombinant mAb
IsotypeMouse IgG1 D265A, κ
Isotype ControlInvivo mouse IgG1 isotype control (D265A)
Applicationin vivo PD-L1 blockade
ReactivityMs
PurificationProtein G
ConcentrationLot specific* (generally 10 to 20 mg/ml)*
Endotoxin<1EU/mg
ConjugationUnconjugated
Physical AppearanceLiquid
Storage Buffer

PBS pH7.4, containing no preservative

Stability & Storage

2 to 8 °C for 2 weeks under sterile conditions;

-20 °C for 3 months under sterile conditions; 

-80 °C for 24 months under sterile conditions.

Please avoid repeated freeze-thaw cycles.

Background

This antibody recognizes the same epitope as clone 10F.9G2. Programmed death-ligand 1 (PD-L1) also known as cluster of differentiation 274 (CD274) or B7 homolog 1 (B7-H1) is a protein that in humans is encoded by the CD274 gene. Programmed death-ligand 1 (PD-L1) is a 40kDa type 1 transmembrane protein that has been speculated to play a major role in suppressing the adaptive arm of immune systems during particular events such as pregnancy, tissue allografts, autoimmune disease and other disease states such as hepatitis. The binding of PD-L1 to the inhibitory checkpoint molecule PD-1 transmits an inhibitory signal based on interaction with phosphatases (SHP-1 or SHP-2) via Immunoreceptor Tyrosine-Based Switch Motif (ITSM). This reduces the proliferation of antigen-specific T-cells in lymph nodes, while simultaneously reducing apoptosis in regulatory T cells (anti-inflammatory, suppressive T cells) - further mediated by a lower regulation of the gene Bcl-2. Upregulation of PD-L1 on immune cells (especially myeloid cells) can also lead to formation of an immunosuppressive environment in a highly localized manner that also allow the cancer cells to proliferate.

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